ClinGen Allele Registry
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Canonical Allele Identifier:
CA25066759
Gene: LINC02238
HGNC
NCBI
Linked Data
dbSNP Id:
rs12145291
gnomAD v2:
1-74161795-T-C
gnomAD v3:
1-73696112-T-C
gnomAD v4:
1-73696112-T-C
MyVariant Identifiers:
chr1:g.74161795T>C (hg19)
chr1:g.73696112T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.73696112T>C , CM000663.2:g.73696112T>C
GRCh38
NC_000001.10:g.74161795T>C , CM000663.1:g.74161795T>C
GRCh37
NC_000001.9:g.73934383T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_146300.1:n.99-3639T>C
Search 100 bp 5'
Search 100 bp 3'